chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2113066323113066324TC52GENIChomozygous109982704
2113066803113066804TC53GENIChomozygous109982705
2113066860113066861CT61GENIChomozygous109982706
2113067598113067599GA48GENIChomozygous109982707
2113068110113068111TC82GENIChomozygous109982708
2113068219113068220AG82GENIChomozygous109982709
2113068343113068344TC72GENIChomozygous109982710
2113068848113068849AG71GENIChomozygous109982711
2113069101113069102GA101GENIChomozygous109982712
2113069163113069164TG75GENIChomozygous109982713
2113069344113069345TC70GENICpossibly homozygous109982714
2113069446113069447GA73GENIChomozygous109982715
2113070560113070561CT66GENIChomozygous109982716
2113070851113070852CA110GENIChomozygous109982717